Genetic manipulation of single neurons in vivo reveals specific roles of flamingo in neuronal morphogenesis

被引:68
作者
Sweeney, NT
Li, WJ
Gao, FB [1 ]
机构
[1] Univ Calif San Francisco, Gladstone Neurol Dis, San Francisco, CA 94141 USA
[2] Univ Calif San Francisco, Program Neurosci, San Francisco, CA 94141 USA
[3] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94141 USA
[4] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94141 USA
基金
美国国家科学基金会;
关键词
Drosophila; dendrites; morphogenesis; flamingo; EGF motif;
D O I
10.1006/dbio.2002.0702
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To study the roles of intracellular factors in neuronal morphogenesis, we used the mosaic analysis with a repressible cell marker (MARCM) technique to visualize identifiable single multiple dendritic (MD) neurons in living Drosophila larvae. We found that individual neurons in the peripheral nervous system (PNS) developed clear morphological polarity and diverse dendritic branching patterns in larval stages. Each MD neuron in the same dorsal cluster developed a unique dendritic field, suggesting that they have specific physiological functions. Single-neuron analysis revealed that Flamingo did not affect the general dendritic branching patterns in postmitotic neurons. Instead, Flamingo limited the extension of one or more dorsal dendrites without grossly affecting lateral branches. The dendritic overextension phenotype was partially conferred by the precocious initiation of dorsal dendrites in flamingo mutant embryos. In addition, Flamingo is required cell autonomously to promote axonal growth and to prevent premature axonal branching of PNS neurons. Our molecular analysis also indicated that the amino acid sequence near the first EGF motif is important for the proper localization and function of Flamingo. These results demonstrate that Flamingo plays a role in early neuronal differentiation and exerts specific effects on dendrites and axons. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:76 / 88
页数:13
相关论文
共 56 条
[1]   Ripped pocket and pickpocket, novel Drosophila DEG/ENaC subunits expressed in early development and in mechanosensory neurons [J].
Adams, CM ;
Anderson, MG ;
Motto, DG ;
Price, MP ;
Johnson, WA ;
Welsh, MJ .
JOURNAL OF CELL BIOLOGY, 1998, 140 (01) :143-152
[2]   MORPHOLOGICAL-DIFFERENTIATION OF THE EMBRYONIC PERIPHERAL NEURONS IN DROSOPHILA [J].
BODMER, R ;
JAN, YN .
ROUXS ARCHIVES OF DEVELOPMENTAL BIOLOGY, 1987, 196 (02) :69-77
[3]   NEUROGENESIS OF THE PERIPHERAL NERVOUS-SYSTEM IN DROSOPHILA EMBRYOS - DNA-REPLICATION PATTERNS AND CELL LINEAGES [J].
BODMER, R ;
CARRETTO, R ;
JAN, YN .
NEURON, 1989, 3 (01) :21-32
[4]   Establishment of neuronal polarity: lessons from cultured hippocampal neurons [J].
Bradke, F ;
Dotti, CG .
CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (05) :574-581
[5]  
BRAND AH, 1993, DEVELOPMENT, V118, P401
[6]   Sequoia, a tramtrack-related zinc finger protein, functions as a pan-neural regulator for dendrite and axon morphogenesis in Drosophila [J].
Brenman, JE ;
Gao, FB ;
Jan, LY ;
Jan, YN .
DEVELOPMENTAL CELL, 2001, 1 (05) :667-677
[7]  
BREWSTER R, 1995, DEVELOPMENT, V121, P2923
[8]   Slit proteins: key regulators of axon guidance, axonal branching, and cell migration [J].
Brose, K ;
Tessier-Lavigne, M .
CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (01) :95-102
[9]  
Campos-Ortega J. A., 1997, The Embryonic Development of Drosophila melanogaster, Vsecond
[10]   Postsynaptic CPG15 promotes synaptic maturation and presynaptic axon arbor elaboration in vivo [J].
Cantallops, I ;
Haas, K ;
Cline, HT .
NATURE NEUROSCIENCE, 2000, 3 (10) :1004-1011